➤ Directing multiple competing clinical projects from inception to completion, owning strategic planning and delivery.➤ Independently identifying and researching process improvements to drive efficiency, accuracy, and data precision.➤ Continually leveraging dynamic, servant leadership to empower and facilitate the success of clinical investigations.➤ Leading high-impact change management techniques to streamline workflow, processes, and research outcomes.➤ Performing site qualification, site initiation, interim monitoring, and close-out visits to ensure regulatory compliance.➤ Driving protocol compliance, reviewing the accurate completion of informed consent procedures and data entry.➤ Ensuring accurate data and interpreting it to identify and resolve protocol deviations and risks to subject safety.➤ Evaluating study protocol execution at the site level while also evaluating site staff performance and processes.➤ Successfully conducting thorough audits of essential regulatory documents to ensure completements and accuracy.

➤ Originally came onboard as a project specialist before receiving a series of promotions due to exceptional performance.➤ Acted as an expert in monitoring and managing clinical investigative sites, spearheading the functions of 200+ staff.➤ Effectively trained, mentored, and assessed monitors to empower and facilitate their success, accuracy, and performance.➤ Demonstrated proficiency in all aspects of monitoring, co-monitoring, and managing challenging investigative sites.➤ Built and developed top-performing project teams, bolstered sponsor relationships, and developed recruiting plans.